Literature DB >> 35845146

Integrating Au and ZnO nanoparticles onto graphene nanosheet for enhanced sonodynamic therapy.

Fei Wang1, Boyu Wang2, Wei You2, Guang Chen2, Ye-Zi You2.   

Abstract

Sonodynamic therapy has attracted widespread attention for cancer treatment because of its noninvasiveness and high tissue-penetration ability. Generally, ultrasound irradiation of sonosensitizers produces separated electrons (e-) and holes (h+), which inhibits cancer by producing reactive oxygen species (ROS). However, the separated electrons (e-) and holes (h+) could easily recombine, lowering the yield of ROS and hindering the application of sonodynamic therapy (SDT). Herein, we present a highly efficient sonosensitizer system for enhanced sonodynamic therapy built on reduced graphene oxide (rGO) nanosheets, bridged ZnO and Au nanoparticles, coated with polyvinyl pyrrolidone (PVP). The ultrasound irradiation activates ZnO nanoparticles to generate separated electron-hole (e--h+) pairs, and the rGO nanosheets facilitate electron transfer from ZnO to Au nanoparticles because of the narrow band gap of rGO, which could efficiently restrain the recombination of the e--h+ pairs, thereby significantly augmenting the production of ROS to kill cancer cells, such as U373MG, HeLa, and CT26 cells. Moreover, rGO nanosheets integrated with Au nanoparticles could catalyze the endogenous decomposition of H2O2 into O2, which can alleviate hypoxic tumor microenvironment (TME). Therefore, the rational design of Au-rGO-ZnO@PVP nanomaterials can not only improve the efficiency of sonodynamic therapy, but also mitigate the hypoxic tumor microenvironment, which would provide a new perspective in the development of efficient sonosensitizers. Electronic Supplementary Material: Supplementary material (the UV-vis-NIR absorption spectra of the DPBF and the RhB, biological effect assessment of the Au-rGO-ZnO@PVP, and the inhibition rate of tumor under different treatments during the animal study) is available in the online version of this article at 10.1007/s12274-022-4599-5. © Tsinghua University Press 2022.

Entities:  

Keywords:  reactive oxygen species; reduced graphene oxide; sonodynamic therapy; tumor

Year:  2022        PMID: 35845146      PMCID: PMC9274620          DOI: 10.1007/s12274-022-4599-5

Source DB:  PubMed          Journal:  Nano Res        ISSN: 1998-0000            Impact factor:   10.269


Integrating Au and ZnO nanoparticles onto graphene nanosheet for enhanced sonodynamic therapy
  38 in total

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Journal:  Adv Mater       Date:  2013-02-15       Impact factor: 30.849

Review 2.  Treating cancer with sonodynamic therapy: a review.

Authors:  David Costley; Conor Mc Ewan; Colin Fowley; Anthony P McHale; Jordan Atchison; Nikolitsa Nomikou; John F Callan
Journal:  Int J Hyperthermia       Date:  2015-01-13       Impact factor: 3.914

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4.  Micro/Nanoparticle-Augmented Sonodynamic Therapy (SDT): Breaking the Depth Shallow of Photoactivation.

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Journal:  Adv Mater       Date:  2016-07-06       Impact factor: 30.849

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Authors:  Chen Dai; Shengjian Zhang; Zhuang Liu; Rong Wu; Yu Chen
Journal:  ACS Nano       Date:  2017-08-28       Impact factor: 15.881

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8.  Multifunctional Metal-Organic Framework Nanoprobe for Cathepsin B-Activated Cancer Cell Imaging and Chemo-Photodynamic Therapy.

Authors:  Jintong Liu; Lei Zhang; Jianping Lei; Hong Shen; Huangxian Ju
Journal:  ACS Appl Mater Interfaces       Date:  2017-01-12       Impact factor: 9.229

9.  Multifunctional sonosensitizers in sonodynamic cancer therapy.

Authors:  Subin Son; Ji Hyeon Kim; Xianwen Wang; Chuangli Zhang; Shin A Yoon; Jinwoo Shin; Amit Sharma; Min Hee Lee; Liang Cheng; Jiasheng Wu; Jong Seung Kim
Journal:  Chem Soc Rev       Date:  2020-04-27       Impact factor: 54.564

10.  Mitochondria-specific drug release and reactive oxygen species burst induced by polyprodrug nanoreactors can enhance chemotherapy.

Authors:  Wenjia Zhang; Xianglong Hu; Qi Shen; Da Xing
Journal:  Nat Commun       Date:  2019-04-12       Impact factor: 14.919

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